(Q35200253)

English

Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids (English)

1 reference

Europe PubMed Central

7 August 2017

Becker muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

Roncuzzi L

1

1 reference

Europe PubMed Central

7 August 2017

Fadda S

2

1 reference

Europe PubMed Central

7 August 2017

Mochi M

3

1 reference

Europe PubMed Central

7 August 2017

Prosperi L

4

1 reference

Europe PubMed Central

7 August 2017

Sangiorgi S

5

1 reference

Europe PubMed Central

7 August 2017

Santamaria R

6

1 reference

Europe PubMed Central

7 August 2017

Sbarra D

7

1 reference

Europe PubMed Central

7 August 2017

Besana D

8

1 reference

Europe PubMed Central

7 August 2017

Morandi L

9

1 reference

Europe PubMed Central

7 August 2017

Rocchi M

10

1 reference

Europe PubMed Central

7 August 2017

language of work or name

0 references

publication date

1 March 1985

1 reference

Europe PubMed Central

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

7 August 2017

37

1 reference

Europe PubMed Central

7 August 2017

407-417

1 reference

Europe PubMed Central

7 August 2017

2

1 reference

Europe PubMed Central

7 August 2017

An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

Fluorescence analysis of late DNA replication in human metaphase chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684576

13 July 2018

A simple method for fusing human lymphocytes with rodent cells in monolayer by polyethylene glycol

1 reference

https://pubmed.ncbi.nlm.nih.gov/2984927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical trial in Duchenne dystrophy. I. The design of the protocol

1 reference

https://pubmed.ncbi.nlm.nih.gov/2984927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2984927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis for the clinical diversity of beta thalassaemia in Cypriots

1 reference

https://pubmed.ncbi.nlm.nih.gov/2984927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localisation of gene for Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2984927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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